GB765642A - Improvements in or relating to silicone-alkyd resins - Google Patents
Improvements in or relating to silicone-alkyd resinsInfo
- Publication number
- GB765642A GB765642A GB8613/55A GB861355A GB765642A GB 765642 A GB765642 A GB 765642A GB 8613/55 A GB8613/55 A GB 8613/55A GB 861355 A GB861355 A GB 861355A GB 765642 A GB765642 A GB 765642A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- alcohol
- acid
- dicarboxylic
- trimethylolethane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/445—Block-or graft-polymers containing polysiloxane sequences containing polyester sequences
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
A silicone-alkyd resin consists essentially of the reaction product of (1) 5 to 60 per cent (by weight) of an organosilicon compound of the general formula RnSiXmO4-n-m/2, wherein each R is a monovalent hydrocarbon or halogenated hydrocarbon radical, each X is a halogen atom, alkoxy or hydroxy radical, n has an average value of 1 to 2 and m has an average value of 0.05 to 3; (2) 10 to 35 per cent of alcohol composed of 20 to 100 per cent by weight, calculated on the total alcohol content, of trimethylolethane, 0 to 50 per cent of a dihydric alcohol and 0 to 30 per cent of another trihydric alcohol; and (3) 20 to 60 per cent of a dicarboxylic acid, anhydride or lower alkyl ester (i.e. containing less than 9 carbon atoms) thereof. The preferred method of making the resins comprises the single stage reaction of (1) 5 to 60 per cent of the organosilicon compound, (2) 10 to 35 per cent of alcohol composed of 50 to 100 per cent of trimethylolethane and 0 to 50 per cent of a dihydric alcohol, and (3) 20 to 60 per cent of a lower alkyl ester of a dicarboxylic acid, at 100 DEG to 250 DEG C. until the desired viscosity is obtained. The reaction may be effected in the presence of a catalyst such as magnesium acetate or perfluoroglutaric acid. Reactants specified are: (1) dimethyldichloro-, dibutyldi-isopropoxy-, phenylmethyldichloro, divinyldibutoxy-, tolyltriethoxy, cyclohexyl-trimethoxy-, phenylmethyldibromo-, (trifluoromethylphenyl) methyldichloro-, chlorophenyltriethoxy-, bromoxenyltrichloro-, stearylmethyldiethoxy and allylstearyloxydimethoxy-silanes, mixtures and hydrolysates thereof, diphenyl-, phenylmethyl-, dimethyl-, chlorophenylmethyl- and octadecylmethyl-silanediols; (2) ethylene glycol, neopentylglycol and glycerine; (3) malonic, adipic, maleic, dimethylmaleic, cyclohexyldicarboxylic, phthalic, terephthalic, isophthalic, naphthalic, stilbene dicarboxylic, diphenic, tolane dicarboxylic and dibenzyl dicarboxylic acids, their anhydrides and alkyl esters containing less than 9 carbon atoms. In a modification up to 50 per cent of (1) may be replaced by a drying oil and/or drying oil acid, e.g. linseed, sardine, soyabean, dehydrated castor, tung, oiticica, perilla, chinawood, hemp seed, poppy seed, safflower, sunflower or walnut oil or acid derived therefrom. The resins may be dissolved in solvents such as acetonyl alcohol, naphtha, isophorone or cresylic acid or solvent mixtures such as diacetone alcohol and butyrolactone; petroleum hydrocarbons, isophorone and methylamylacetate; acetonyl acetone and diacetone alcohol; and C6H5.OCH2.CH2.OOC.CH3 and diacetone alcohol, and used for coating metal surfaces, particularly fine wire. Examples are given. Specification 663,599 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US765642XA | 1954-05-28 | 1954-05-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB765642A true GB765642A (en) | 1957-01-09 |
Family
ID=22132814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8613/55A Expired GB765642A (en) | 1954-05-28 | 1955-03-24 | Improvements in or relating to silicone-alkyd resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB765642A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0075326A1 (en) * | 1981-09-23 | 1983-03-30 | Dow Corning Corporation | Non-precondensed silicone-alkyd resins and a method for their preparation |
-
1955
- 1955-03-24 GB GB8613/55A patent/GB765642A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0075326A1 (en) * | 1981-09-23 | 1983-03-30 | Dow Corning Corporation | Non-precondensed silicone-alkyd resins and a method for their preparation |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2160532A (en) | Esters | |
US2048799A (en) | Silicon esters of modified polyhydroxy alcohols | |
US2618616A (en) | Modified alkyd resins and composi | |
US2892780A (en) | Alkyd gels and compositions containing the same | |
US2091965A (en) | Phenol resin ester and method of preparing | |
US2627508A (en) | Long oil alkyd resins | |
US2516309A (en) | Unsaturated alkyd casting resins | |
US2469371A (en) | Process of reacting glyceride oils | |
US2454862A (en) | Product and process of reacting alkenyl succinic esters with sulfur | |
US2320724A (en) | Method of treating styrene-unsaturated dicarboxylic acid resins | |
US4045391A (en) | Process for preparing low viscosity fatty acid-modified polyesters | |
US3010945A (en) | Polymerizing vinyl cyclic acetals with cobaltous salts of dicarboxylic acid half-esters | |
GB765642A (en) | Improvements in or relating to silicone-alkyd resins | |
US2558025A (en) | Polyester drying oil | |
US3196118A (en) | Coating compositions containing an amine and a metallic drier | |
US2331169A (en) | Esters of methylol phenols | |
US2476891A (en) | Mtxed esters of polyhydric alcohols | |
US3086949A (en) | Process of converting free carboxylic acid groups in liquid ester coating compositions to half-ester groups with retention of the coating composition in the liquid state | |
US1993828A (en) | Synthetic resin | |
US2907743A (en) | Resinous polyhydric phenols | |
US2895932A (en) | Certain isophthalic and orthophthalic | |
DE1570242A1 (en) | Process for the production of modified polyesters | |
US2890186A (en) | Modified dialkyl fumarate alkyd resin reacted with a vinyl aromatic compound, a vinyl cyanide and an acrylate | |
US2655486A (en) | Tetrahydrophthalic alkyd resins | |
US2006555A (en) | Esters of polycarboxylic acids and their production |